(Q30666798)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11738839%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

review article

1 reference

title

The biological functions of the methyl-CpG-binding protein MeCP2 and its implication in Rett syndrome (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11738839%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

0 references

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11738839%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

Adrian Peter Bird

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11738839%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

author name string

Nan X

series ordinal

1

1 reference

26 June 2017

Bird A

series ordinal

2

1 reference

26 June 2017

1 December 2001

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11738839%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

published in

Brain and Development

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11738839%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

volume

23 Suppl 1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11738839%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

page(s)

S32-7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11738839%20AND%20SRC:MED&resulttype=core&format=json

A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: report of 35 cases

4 December 2019

cites work

1 reference

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7 January 2021

Rett syndrome: confirmation of X-linked dominant inheritance, and localization of the gene to Xq28.

1 reference

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7 January 2021

Linkage analysis in Rett syndrome families suggests that there may be a critical region at Xq28

1 reference

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7 January 2021

Chromosome mapping of Rett syndrome: a likely candidate region on the telomere of Xq

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7 January 2021

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

1 reference

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7 January 2021

Rett syndrome: a surprising result of mutation in MECP2.

1 reference

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7 January 2021

Purification, sequence, and cellular localization of a novel chromosomal protein that binds to methylated DNA

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7 January 2021

Cloning and sequencing of a cDNA encoding DNA methyltransferase of mouse cells

1 reference

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7 January 2021

DNA methyltransferases Dnmt3a and Dnmt3b are essential for de novo methylation and mammalian development

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7 January 2021

Targeted mutation of the DNA methyltransferase gene results in embryonic lethality

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7 January 2021

X Inactivation in the Mouse Embryo Deficient for Dnmt1: Distinct Effect of Hypomethylation on Imprinted and Random X Inactivation

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7 January 2021

Methylation-induced repression--belts, braces, and chromatin

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7 January 2021

Identification of a mammalian protein that binds specifically to DNA containing methylated CpGs.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900333-3

7 January 2021

DNA methylation inhibits transcription indirectly via a methyl-CpG binding protein

1 reference

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7 January 2021

Active repression of methylated genes by the chromosomal protein MBD1

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900333-3

7 January 2021

Dissection of the methyl-CpG binding domain from the chromosomal protein MeCP2

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900333-3

7 January 2021

DNA methylation specifies chromosomal localization of MeCP2.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900333-3

7 January 2021

The solution structure of the domain from MeCP2 that binds to methylated DNA

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900333-3

7 January 2021

Solution structure of the methyl-CpG-binding domain of the methylation-dependent transcriptional repressor MBD1

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900333-3

7 January 2021

Identification and characterization of a family of mammalian methyl-CpG binding proteins

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900333-3

7 January 2021

MeCP2 is a transcriptional repressor with abundant binding sites in genomic chromatin

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900333-3

7 January 2021

Methyl-CpG-binding protein MeCP2 represses Sp1-activated transcription of the human leukosialin gene when the promoter is methylated

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900333-3

7 January 2021

The methyl-CpG binding transcriptional repressor MeCP2 stably associates with nucleosomal DNA

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900333-3

7 January 2021

CpG methylation, chromatin structure and gene silencing-a three-way connection

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900333-3

7 January 2021

Structure of chromatin containing extensively acetylated H3 and H4

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900333-3

7 January 2021

Butyrate suppression of histone deacetylation leads to accumulation of multiacetylated forms of histones H3 and H4 and increased DNase I sensitivity of the associated DNA sequences

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900333-3

7 January 2021

Histone deacetylase: a regulator of transcription

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900333-3

7 January 2021

The many HATs of transcription coactivators

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900333-3

7 January 2021

What's up and down with histone deacetylation and transcription?

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900333-3

7 January 2021

Acetylation: a regulatory modification to rival phosphorylation?

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900333-3

7 January 2021

Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900333-3

7 January 2021

Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complex

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900333-3

7 January 2021

MeCP2 driven transcriptional repression in vitro: selectivity for methylated DNA, action at a distance and contacts with the basal transcription machinery

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900333-3

7 January 2021

Histone deacetylase-independent transcriptional repression by methyl-CpG-binding protein 2.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900333-3

7 January 2021

A component of the transcriptional repressor MeCP1 shares a motif with DNA methyltransferase and HRX proteins

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900333-3

7 January 2021

Mi-2 complex couples DNA methylation to chromatin remodelling and histone deacetylation

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900333-3

7 January 2021

MBD2-MBD3 complex binds to hemi-methylated DNA and forms a complex containing DNMT1 at the replication foci in late S phase

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900333-3

7 January 2021

Mechanism of transcriptional regulation by methyl-CpG binding protein MBD1

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900333-3

7 January 2021

MBD2 is a transcriptional repressor belonging to the MeCP1 histone deacetylase complex

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900333-3

7 January 2021

The minimal repression domain of MBD2b overlaps with the methyl-CpG-binding domain and binds directly to Sin3A

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900333-3

7 January 2021

Biphasic kinetics of the human DNA repair protein MED1 (MBD4), a mismatch-specific DNA N-glycosylase

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900333-3

7 January 2021

The thymine glycosylase MBD4 can bind to the product of deamination at methylated CpG sites

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900333-3

7 January 2021

MED1, a novel human methyl-CpG-binding endonuclease, interacts with DNA mismatch repair protein MLH1

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900333-3

7 January 2021

The DNA repair gene MBD4 (MED1) is mutated in human carcinomas with microsatellite instability

1 reference

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7 January 2021

Somatic frameshift mutations in the MBD4 gene of sporadic colon cancers with mismatch repair deficiency.

1 reference

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7 January 2021

Rett syndrome: analysis of MECP2 and clinical characterization of 31 patients.

1 reference

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7 January 2021

Mutational analysis of the MECP2 gene in Japanese patients with Rett syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900333-3

7 January 2021

Long-read sequence analysis of the MECP2 gene in Rett syndrome patients: correlation of disease severity with mutation type and location.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900333-3

7 January 2021

MECP2 mutation in male patients with non-specific X-linked mental retardation.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900333-3

7 January 2021

Effects of Rett syndrome mutations of the methyl-CpG binding domain of the transcriptional repressor MeCP2 on selectivity for association with methylated DNA

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900333-3

7 January 2021

DNA recognition by the methyl-CpG binding domain of MeCP2.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900333-3

7 January 2021

Treatment of Wilson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900333-3

7 January 2021

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900333-3

7 January 2021

Absence of expression of the FMR-1 gene in fragile X syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900333-3

7 January 2021

Large-scale chromatin unfolding and remodeling induced by VP16 acidic activation domain

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900333-3

7 January 2021

Applications of peptide nucleic acids

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900333-3

7 January 2021

Triplex-directed modification of genes and gene activity

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900333-3

7 January 2021

DNA-like double helix formed by peptide nucleic acid

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900333-3

7 January 2021

Extended DNA-recognition repertoire of peptide nucleic acid (PNA): PNA-dsDNA triplex formed with cytosine-rich homopyrimidine PNA.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900333-3

7 January 2021

Cell penetrating PNA constructs regulate galanin receptor levels and modify pain transmission in vivo

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900333-3

7 January 2021

PNA-dependent gene chemistry: stable coupling of peptides and oligonucleotides to plasmid DNA.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900333-3

7 January 2021

10.1016/S0387-7604(01)00333-3

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11738839%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

1 reference